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Inuloxin E, a New Seco-Eudesmanolide Isolated from Dittrichia viscosa, Stimulating Orobanche cumana Seed Germination.


ABSTRACT: A new sesquiterpenoid belonging to the subgroup seco-eudesmanolides and named inuloxin E was isolated from Dittrichia viscosa, together with the already known sesquiterpenoids inuloxins A-D and ?-costic acid. Inuloxin E was characterized by spectroscopic data (essentially NMR and ESI MS) as 3-methylene-6-(1-methyl-4-oxo-pentyl)-3a,4,7,7a-tetrahydro-3H-benzofuran-2-one. Its relative configuration was determined by comparison with the closely related inuloxin D and chemical conversion of inuloxin E into inuloxin D and by the observed significant correlation in the NOESY spectrum. Both inuloxins D and E induced germination of the parasitic weed Orobanche cumana, but were inactive on the seeds of Orobanche minor and Phelipanche ramosa. The germination activity of some hemisynthetic esters of inuloxin D was also investigated.

SUBMITTER: Masi M 

PROVIDER: S-EPMC6803869 | biostudies-literature | 2019 Sep

REPOSITORIES: biostudies-literature

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Inuloxin E, a New Seco-Eudesmanolide Isolated from <i>Dittrichia viscosa</i>, Stimulating <i>Orobanche cumana</i> Seed Germination.

Masi Marco M   Fernández-Aparicio Mónica M   Zatout Roukia R   Boari Angela A   Cimmino Alessio A   Evidente Antonio A  

Molecules (Basel, Switzerland) 20190925 19


A new sesquiterpenoid belonging to the subgroup seco-eudesmanolides and named inuloxin E was isolated from <i>Dittrichia viscosa</i>, together with the already known sesquiterpenoids inuloxins A-D and α-costic acid. Inuloxin E was characterized by spectroscopic data (essentially NMR and ESI MS) as 3-methylene-6-(1-methyl-4-oxo-pentyl)-3a,4,7,7a-tetrahydro-3<i>H</i>-benzofuran-2-one. Its relative configuration was determined by comparison with the closely related inuloxin D and chemical conversio  ...[more]

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